Works matching IS 00099163 AND DT 1984 AND VI 26 AND IP 3
Results: 34
THIRD NORDIC CONFERENCE Pepsinogen and gastric cancer.
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- Clinical Genetics, 1984, v. 26, n. 3, p. 240, doi. 10.1111/j.1399-0004.1984.tb04377.x
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Endocrine Genetics and Genetics of Growth.
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- Clinical Genetics, 1984, v. 26, n. 3, p. 280, doi. 10.1111/j.1399-0004.1984.tb04396.x
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- Article
Diagnostic transcervical chorionic biopsles in first trimester pregnancies.
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- Clinical Genetics, 1984, v. 26, n. 3, p. 262, doi. 10.1111/j.1399-0004.1984.tb04386.x
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Analysis of a familial 15p + polymorphism: exclusion of Y/15 translocation.
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- Clinical Genetics, 1984, v. 26, n. 3, p. 204, doi. 10.1111/j.1399-0004.1984.tb04368.x
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Fragile sites and chromosome breakpoints in constitutional rearrangements II. Spontaneous abortions, stillbirths and newborns.
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- Clinical Genetics, 1984, v. 26, n. 3, p. 174, doi. 10.1111/j.1399-0004.1984.tb04364.x
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Oro-facio-digital syndromes I and II: radiological methods for diagnosis and the clinical variations.
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- Clinical Genetics, 1984, v. 26, n. 3, p. 178, doi. 10.1111/j.1399-0004.1984.tb04365.x
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FamiIial vascuIar malformations Report of 25 members of one family.
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- Clinical Genetics, 1984, v. 26, n. 3, p. 221, doi. 10.1111/j.1399-0004.1984.tb04371.x
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Experience with transabdominal fine needle biopsy from chorionic villi in the first trimester: an alternative to amniocentesis.
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- Clinical Genetics, 1984, v. 26, n. 3, p. 272, doi. 10.1111/j.1399-0004.1984.tb04392.x
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Hereditary lymphedema: a new combination of symptoms not fitting into present classifications.
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- Clinical Genetics, 1984, v. 26, n. 3, p. 254, doi. 10.1111/j.1399-0004.1984.tb04383.x
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Four cases of the prenatal diagnosis of trisomy 20 mosaicism with a follow up investigation.
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- Clinical Genetics, 1984, v. 26, n. 3, p. 265, doi. 10.1111/j.1399-0004.1984.tb04388.x
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Familial porencephaly.
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- Clinical Genetics, 1984, v. 26, n. 3, p. 236, doi. 10.1111/j.1399-0004.1984.tb04375.x
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Prometaphase chromosome and immunological studies in different derivatives of balanced t(8;14)(p231;q323).
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- Clinical Genetics, 1984, v. 26, n. 3, p. 276, doi. 10.1111/j.1399-0004.1984.tb04394.x
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Two cases of 11p13 interstitial deletion and unusual clinical features.
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- Clinical Genetics, 1984, v. 26, n. 3, p. 247, doi. 10.1111/j.1399-0004.1984.tb04380.x
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Rocker bottom feet.
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- Clinical Genetics, 1984, v. 26, n. 3, p. 258, doi. 10.1111/j.1399-0004.1984.tb04385.x
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The Occurrence of 'Finnish' hereditary diseases in the other Nordic countries.
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- Clinical Genetics, 1984, v. 26, n. 3, p. 269, doi. 10.1111/j.1399-0004.1984.tb04390.x
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Cholesterol ester storage disease in an adult presenting with sea-blue histiocytosis.
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- Clinical Genetics, 1984, v. 26, n. 3, p. 195, doi. 10.1111/j.1399-0004.1984.tb04367.x
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Distal trisomy 14q syndrome; a case report.
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- Clinical Genetics, 1984, v. 26, n. 3, p. 231, doi. 10.1111/j.1399-0004.1984.tb04373.x
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Basement membrane proteins in human amniotic fluid.
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- Clinical Genetics, 1984, v. 26, n. 3, p. 271, doi. 10.1111/j.1399-0004.1984.tb04391.x
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Autosomal recesslve ichthyosis in Norway: II. Sjøgren-Larsson-like ichthyosis without CNS or eye involvement.
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- Clinical Genetics, 1984, v. 26, n. 3, p. 242, doi. 10.1111/j.1399-0004.1984.tb04378.x
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Papers presented at The Third Nordic Conference of Medical Genetics Helsinki, Finland, 17-19 February 1984.
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- Clinical Genetics, 1984, v. 26, n. 3, p. 235, doi. 10.1111/j.1399-0004.1984.tb04374.x
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- Article
Nager's acrofacial dysostosis with thumb duplication: report of a case.
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- Clinical Genetics, 1984, v. 26, n. 3, p. 228, doi. 10.1111/j.1399-0004.1984.tb04372.x
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Unexpected findings at prenatal diagnosis.
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- Clinical Genetics, 1984, v. 26, n. 3, p. 268, doi. 10.1111/j.1399-0004.1984.tb04389.x
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Ankylosing spondylitis is part of a multifactorial syndrome: hereditary multifocal relapsing inflammation (HEMRI).
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- Clinical Genetics, 1984, v. 26, n. 3, p. 187, doi. 10.1111/j.1399-0004.1984.tb04366.x
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Fragile sites and chromosome breakpoints in constitutional rearrangements I. Amniocentesis.
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- Clinical Genetics, 1984, v. 26, n. 3, p. 169, doi. 10.1111/j.1399-0004.1984.tb04363.x
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A 5p;22q reciprocal translocation with a high risk for segregation of unbalanced offspring.
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- Clinical Genetics, 1984, v. 26, n. 3, p. 252, doi. 10.1111/j.1399-0004.1984.tb04382.x
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First trimester biopsies of chorionic villi for prenatal diagnosis: experience of two laboratories.
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- Clinical Genetics, 1984, v. 26, n. 3, p. 263, doi. 10.1111/j.1399-0004.1984.tb04387.x
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Scoliosis and retinal changes in a G syndrome carrier.
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- Clinical Genetics, 1984, v. 26, n. 3, p. 274, doi. 10.1111/j.1399-0004.1984.tb04393.x
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Prader-Willi syndrome in a child with a balanced (X;15) de novo translocation.
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- Clinical Genetics, 1984, v. 26, n. 3, p. 245, doi. 10.1111/j.1399-0004.1984.tb04379.x
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Occurrences of methylmalonic aciduria and Hartnup disorder in the same family.
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- Clinical Genetics, 1984, v. 26, n. 3, p. 216, doi. 10.1111/j.1399-0004.1984.tb04370.x
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Alpers' disease.
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- Clinical Genetics, 1984, v. 26, n. 3, p. 256, doi. 10.1111/j.1399-0004.1984.tb04384.x
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Hydrops fetalis: a new aspect of trisomy 18.
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- Clinical Genetics, 1984, v. 26, n. 3, p. 238, doi. 10.1111/j.1399-0004.1984.tb04376.x
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Meningocele in a boy with trisomy 13.
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- Clinical Genetics, 1984, v. 26, n. 3, p. 278, doi. 10.1111/j.1399-0004.1984.tb04395.x
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Familial partial monosomy 5p and trisomy 5q; three cases due to paternal pericentric inversion 5 (p151q333).
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- Clinical Genetics, 1984, v. 26, n. 3, p. 209, doi. 10.1111/j.1399-0004.1984.tb04369.x
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Semi-lethal bone dysplasia in three sibs: a new genetic disorder.
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- Clinical Genetics, 1984, v. 26, n. 3, p. 249, doi. 10.1111/j.1399-0004.1984.tb04381.x
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